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Topoisomerase IIβ Binding Protein 1 c.*229C>T (rs115160714) Gene Polymorphism and Endometrial Cancer Risk

TopBP1 (topoisomerase IIβ binding protein 1) protein is involved in DNA replication, DNA damage checkpoint response and transcriptional regulation. In this study we investigated whether alterations in the TopBP1 gene can influence the risk of endometrial cancer. We examined the association between f...

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Autores principales: Forma, Ewa, Wójcik-Krowiranda, Katarzyna, Jóźwiak, Paweł, Szymczyk, Agnieszka, Bieńkiewicz, Andrzej, Bryś, Magdalena, Krześlak, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4062805/
https://www.ncbi.nlm.nih.gov/pubmed/24346708
http://dx.doi.org/10.1007/s12253-013-9737-7
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author Forma, Ewa
Wójcik-Krowiranda, Katarzyna
Jóźwiak, Paweł
Szymczyk, Agnieszka
Bieńkiewicz, Andrzej
Bryś, Magdalena
Krześlak, Anna
author_facet Forma, Ewa
Wójcik-Krowiranda, Katarzyna
Jóźwiak, Paweł
Szymczyk, Agnieszka
Bieńkiewicz, Andrzej
Bryś, Magdalena
Krześlak, Anna
author_sort Forma, Ewa
collection PubMed
description TopBP1 (topoisomerase IIβ binding protein 1) protein is involved in DNA replication, DNA damage checkpoint response and transcriptional regulation. In this study we investigated whether alterations in the TopBP1 gene can influence the risk of endometrial cancer. We examined the association between five single nucleotide polymorphisms (rs185903567, rs116645643, rs115160714, rs116195487, and rs112843513) located in the 3′UTR region of the TopBP1 gene and endometrial cancer risk as well as allele-specific gene expression. One hundred twenty-one endometrial cancer patients were genotyped for these SNPs. Allele-specific TopBP1 mRNA and protein expressions were determined by real time PCR and western blotting methods, respectively. Only one SNP (rs115160714) showed an association with endometrial cancer. Compared to homozygous common allele carriers, heterozygous for the T variant had significantly increased risk of endometrial cancer [adjusted odds ratio (OR) = 5.59, 95 % confidence interval (CI): 1.96–15.91, p = 0.0003]. Mean TopBP1 mRNA and protein expression were higher in the individuals with the CT genotype. There was a significant association between the rs115160714 and tumor grade and FIGO classification. Most carriers of minor allele had a high grade tumors (G3) classified as FIGO III/IV. The results of our study raise a possibility that a genetic variation of TopBP1 may be implicated in the etiology of endometrial cancer.
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spelling pubmed-40628052014-06-25 Topoisomerase IIβ Binding Protein 1 c.*229C>T (rs115160714) Gene Polymorphism and Endometrial Cancer Risk Forma, Ewa Wójcik-Krowiranda, Katarzyna Jóźwiak, Paweł Szymczyk, Agnieszka Bieńkiewicz, Andrzej Bryś, Magdalena Krześlak, Anna Pathol Oncol Res Research TopBP1 (topoisomerase IIβ binding protein 1) protein is involved in DNA replication, DNA damage checkpoint response and transcriptional regulation. In this study we investigated whether alterations in the TopBP1 gene can influence the risk of endometrial cancer. We examined the association between five single nucleotide polymorphisms (rs185903567, rs116645643, rs115160714, rs116195487, and rs112843513) located in the 3′UTR region of the TopBP1 gene and endometrial cancer risk as well as allele-specific gene expression. One hundred twenty-one endometrial cancer patients were genotyped for these SNPs. Allele-specific TopBP1 mRNA and protein expressions were determined by real time PCR and western blotting methods, respectively. Only one SNP (rs115160714) showed an association with endometrial cancer. Compared to homozygous common allele carriers, heterozygous for the T variant had significantly increased risk of endometrial cancer [adjusted odds ratio (OR) = 5.59, 95 % confidence interval (CI): 1.96–15.91, p = 0.0003]. Mean TopBP1 mRNA and protein expression were higher in the individuals with the CT genotype. There was a significant association between the rs115160714 and tumor grade and FIGO classification. Most carriers of minor allele had a high grade tumors (G3) classified as FIGO III/IV. The results of our study raise a possibility that a genetic variation of TopBP1 may be implicated in the etiology of endometrial cancer. Springer Netherlands 2013-12-18 2014 /pmc/articles/PMC4062805/ /pubmed/24346708 http://dx.doi.org/10.1007/s12253-013-9737-7 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Research
Forma, Ewa
Wójcik-Krowiranda, Katarzyna
Jóźwiak, Paweł
Szymczyk, Agnieszka
Bieńkiewicz, Andrzej
Bryś, Magdalena
Krześlak, Anna
Topoisomerase IIβ Binding Protein 1 c.*229C>T (rs115160714) Gene Polymorphism and Endometrial Cancer Risk
title Topoisomerase IIβ Binding Protein 1 c.*229C>T (rs115160714) Gene Polymorphism and Endometrial Cancer Risk
title_full Topoisomerase IIβ Binding Protein 1 c.*229C>T (rs115160714) Gene Polymorphism and Endometrial Cancer Risk
title_fullStr Topoisomerase IIβ Binding Protein 1 c.*229C>T (rs115160714) Gene Polymorphism and Endometrial Cancer Risk
title_full_unstemmed Topoisomerase IIβ Binding Protein 1 c.*229C>T (rs115160714) Gene Polymorphism and Endometrial Cancer Risk
title_short Topoisomerase IIβ Binding Protein 1 c.*229C>T (rs115160714) Gene Polymorphism and Endometrial Cancer Risk
title_sort topoisomerase iiβ binding protein 1 c.*229c>t (rs115160714) gene polymorphism and endometrial cancer risk
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4062805/
https://www.ncbi.nlm.nih.gov/pubmed/24346708
http://dx.doi.org/10.1007/s12253-013-9737-7
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